Cleanrooms: Designed to deliver, guaranteed.

Designed to Deliver Certainty

With a tailored CleanFit plan (and its “design to deliver” approach), your clean space is certain be the most reliable and advanced, with the costs certain to come in as planned.

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Certainty of CleanFit

Designed to Deliver Continuity

The same expert team is with you from design through installation, and beyond, and they are financially committed to your schedule and costs. No need to read-in or manage multiple contractors and risk miscommunication.

One Team, No Compromises

Designed to Deliver Collaboration

An easy-to-access and share CleanFit plan removes any distinction between external and internal resources – we’re one team, with one goal, and a clear window into progress.

Open, Often
Communication

Controlled environments that are designed and assembled to precise specifications

Clean Rooms

Learn more about our clean room expertise.

Cold Rooms

Learn more about our cold room expertise.

Dry Rooms

Learn more about our dry room expertise.

The CleanFit Process

CleanFit accelerates the design to installation process and is what enables CleanSpace to offer timeline and budget guarantees.

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CleanSpace Insights

Improve the speed and efficiency, provoke dialogue for alignment and consider key decision points as you prepare for your next project.

Softwall vs. Hardwall

There are two broad categories of cleanrooms. Softwall cleanrooms, often regarded as more temporary solutions, consist of a prefabricated frame and walls made from flexible vinyl sheets.

What is a BSL Cleanroom?

The Biological Safety Level (BSL) serves as a system of biocontainment designation, essential for safeguarding personnel against potential pathogenic exposure in research and manufacturing environments. This system outlines specific requirements for protecting those working in these settings. It’s crucial to note the revision of the Biological Safety Level (BSL) standards in the Biosafety in Microbiological and Biomedical Laboratories (BMBL) in 2020. This update brought about the 6th edition of these standards and included several key updates.

How to Clean Your Cleanroom

Maintaining a pristine environment is paramount in scientific research, semiconductor manufacturing, and additional, highly regulated industries.

GMP & Modular Cleanrooms

The acronym GMP stands for Good Manufacturing Practice. Its origins lie in the tragedies of the 1950s and 1960s, where poor manufacturing practices led to fatalities and congenital disabilities in pharmaceutical products.

Sustainability and Reduced Environmental Impact of Modular Cleanrooms

Once upon a time, building a Cleanroom was an environmental nightmare. Traditional “stick-built” methods relied heavily on resource-intensive materials like brick, mortar, and concrete, leaving a trail of extraction and emissions in their wake.

What are ATMPs?

The term Advanced Therapy Medicinal Products (ATMPs) officially emerged in 2007, with the adoption of Regulation (EC) No 1394/2007 by the European Commission. This regulation established a legal framework for these innovative therapies in the European Union.

Cleanrooms: Designed to deliver, guaranteed.

Designed to Deliver Certainty

Designed to Deliver Continuity

Designed to Deliver Collaboration